A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3815



Internal ID15538542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:103889893..103911332hg38UCSC Ensembl
OuterchrX:103144814..103166252hg19UCSC Ensembl
OuterchrX:103031470..103052908hg18UCSC Ensembl
OuterchrX:102950959..102972397hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3821440
hg1921439
hg1821439
hg1721439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7018
Supporting Variants
SamplesNA12878
Known GenesMIR1256
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv3815
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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